Canonical Allele Identifier: CA830561639

Gene: SERPINE1

Linked Data

• dbSNP Id: rs1183833436
• gnomAD v3: 7-101131469-T-C
• gnomAD v4: 7-101131469-T-C
• MyVariant Identifiers: chr7:g.100774750T>C (hg19) ; chr7:g.101131469T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.101131469T>C , CM000669.2:g.101131469T>C	GRCh38
NC_000007.13:g.100774750T>C , CM000669.1:g.100774750T>C	GRCh37
NC_000007.12:g.100561470T>C	NCBI36
NG_013213.1:g.9372T>C , LRG_597:g.9372T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000223095.5:c.506-406T>C MANE Select	ENSP00000223095.4:n.506-406T>C
ENST00000223095.4:c.506-406T>C	ENSP00000223095.4:n.506-406T>C
NM_000602.4:c.506-406T>C , LRG_597t1:c.506-406T>C	NP_000593.1:n.506-406T>C
NM_000602.5:c.506-406T>C MANE Select	NP_000593.1:n.506-406T>C
NM_001386456.1:c.254-406T>C	NP_001373385.1:n.254-406T>C
NM_001386457.1:c.506-406T>C	NP_001373386.1:n.506-406T>C
NM_001386458.1:c.506-406T>C	NP_001373387.1:n.506-406T>C
NM_001386459.1:c.506-406T>C	NP_001373388.1:n.506-406T>C
NM_001386460.1:c.506-406T>C	NP_001373389.1:n.506-406T>C
NM_001386461.1:c.506-406T>C	NP_001373390.1:n.506-406T>C
NM_001386462.1:c.305-406T>C	NP_001373391.1:n.305-406T>C
NM_001386463.1:c.500-406T>C	NP_001373392.1:n.500-406T>C
NM_001386464.1:c.506-406T>C	NP_001373393.1:n.506-406T>C
NM_001386465.1:c.506-406T>C	NP_001373394.1:n.506-406T>C
NM_001386466.1:c.530-406T>C	NP_001373395.1:n.530-406T>C